Novel Partially Fluorinated Copolymers: Evidence of the Effect of Fluorine on the Reactivity of the Unfluorinated Comonomer Units
β Scribed by Massimo Lazzari; Dominique Scalarone; Valter Castelvetro; Francesca Signori; Oscar Chiantore
- Book ID
- 102496297
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 140 KB
- Volume
- 26
- Category
- Article
- ISSN
- 1022-1336
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β¦ Synopsis
Abstract
Summary: A conventional freeβradical polymerization of vinyl or propenyl ethers with acrylic or methacrylic monomers with fluorine substitution either in the main chain or in the ester groups has permitted us to obtain a series of copolymers with substantially different fluorine contents and distributions to be obtained. Such copolymers were considered as model compounds to offer new valuable insights as to the influence of fluorinated moieties on the overall stability and, more specifically, on their reactivity with atmospheric oxygen under environmentalβlike conditions. Depending on the relative position of the fluorine atoms with respect to the common active center of oxidation, the influence ranges from a simple slowing down of the process to a complete redirection towards an otherwise secondary mechanism of oxidation.
FTβIR spectra of the carbonyl region of three novel fluorinated copolymers after oxidation.
imageFTβIR spectra of the carbonyl region of three novel fluorinated copolymers after oxidation.
π SIMILAR VOLUMES
## Abstract Nylon 610/65F and nylon 610/65 copolymers were prepared by melt polycondensation from the diethylester of sebacic acid (10) and hexafluoroglutaric acid (5F) or glutaric acid (5) with hexamethylene diamine (6). Reduced specific viscosities of nylon 610/65F were lower than those of nylon